Quality Assurance Supervisor

ph3Quality Assurance Supervisor /h3 /brpAzienda : Phibro Llc Tipo Lavoro : Full Time Italy JobCopilot will tailor your resume and auto-fill the application /p /brh3Descrizione Lavoro - Quality Assurance Supervisor /h3 /brpbAbout Phibro Animal Health Corporation /b /p /brpbPhibro Animal Health Corporation /b is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. /p /brpPhibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide. /p /brpAt Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. /p /brpIf you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. /p /brpTheQuality Assurance Supervisoris an integral part of our Quality Assuranceteam based out of our Medolla, Italysite. /p /brh3Position Details /h3 /brpEDUCATIONbr/Master's degree in a technical-scientific field (Pharmaceutical Chemistry, Medicine, Veterinary, Biology, Chemistry, Pharmacy)br/Esame di stato is requiredbr/EXPERIENCEbr/Minimum of 5 years’ experience in a similar role, ideally in a pharmaceutical manufacturing facilitybr/Strong knowledge of GMP regulations and quality management systemsbr/Experience with regulatory, client and self-inspections auditsbr/Eligible for Qualified Person rolebr/RESPONSIBILITIESbr/Ensure effective monitoring of production processes according to European and Phibro Quality Standards and EU directives and regulationsbr/Ensure the execution of periodic report (Product Quality Review) on the manufactured products and the GMP self-inspectionbr/Manage deviations (generation, investigation, impact, reporting and approval)br/Review of Quality Control (QC) out of specification results and investigationsbr/Review of quality acceptance criteria for raw materials, intermediates products, and finished productsbr/Coordinates and manage periodic audit with Regulatory and Health Authoritiesbr/Ensure that all SOPs and other related documents follow GMP and Phibro Quality Systems. He/she is responsible for site GMP documentation controlbr/Provide quality direction and manage the implementation of changes for critical company systems, according to the "change control" procedurebr/Manage deviations and non-conformities, ensuring the quality of the finished product and verifying the efficacy of the relative corrective actionsbr/Manage customer complaints with related investigation, corrective activities, response and complaint closurebr/Coordinate the activities to support the management of supplier qualification and approve the related Quality Agreement (where necessary)br/Review and approve qualification/validation protocols and reportsbr/Knowledge of root cause analysis methodology and Quality Risk Managementbr/Collaborates in the supervision of the general hygiene conditions of the premises and pest monitoring activities for which he/she is responsiblebr/Provide information for, and complete, as necessary customer by mail surveys, audits, and inquiriesbr/As Qualified Person, the quality assurance lead is responsible to ensure compliance with Regulation (EU) 2019/6 on veterinary medicinal products, applicable EU GMP requirements, marketing authorizations, manufacturing authorizations, and relevant national implementing legislation.br/Provide quality oversight of feed additive manufacturing activities and ensure compliance with applicable feed and feed-additive regulations, site licenses, and quality standards.br/Ensure appropriate segregation between veterinary medicinal product GMP activities and feed additive quality requirements where applicable.br/CORE COMPETENCIESbr/Excellent problem-solving and decision-making skillsbr/Good team building and collaboration both on-site and with teams remotelybr/Promote a culture of continuous learning and development for the site quality organizationbr/Improve on-site understanding of GMP’s through good quality programs, procedures, and trainingbr/Ability to prioritize different activities and manage multiple projectsbr/Strong communication skillsbr/Fluent in spoken and written English and Italian /p /brpbPhibro is an Equal Opportunity Employer /b /p /brpAll qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. /p /brpbBusiness Unit:Animal Health Mineral Nutrition /bbr/bDivision:Animal Health Nutrition /bbr/bDepartment:Quality Assurance /bbr/bLocation:Medolla, Italy /bbr/bWork Schedule:Monday - Friday (40 Hours) /b /p /p #J-18808-Ljbffr